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Trophic network architecture of root-associated bacterial communities determines pathogen invasion and plant health
Host-associated bacterial communities can function as an important line of defence against pathogens in animals and plants. Empirical evidence and theoretical predictions suggest that species-rich communities are more resistant to pathogen invasions. Yet, the underlying mechanisms are unclear. Here,...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Pub. Group
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4598729/ https://www.ncbi.nlm.nih.gov/pubmed/26400552 http://dx.doi.org/10.1038/ncomms9413 |
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author | Wei, Zhong Yang, Tianjie Friman, Ville-Petri Xu, Yangchun Shen, Qirong Jousset, Alexandre |
author_facet | Wei, Zhong Yang, Tianjie Friman, Ville-Petri Xu, Yangchun Shen, Qirong Jousset, Alexandre |
author_sort | Wei, Zhong |
collection | PubMed |
description | Host-associated bacterial communities can function as an important line of defence against pathogens in animals and plants. Empirical evidence and theoretical predictions suggest that species-rich communities are more resistant to pathogen invasions. Yet, the underlying mechanisms are unclear. Here, we experimentally test how the underlying resource competition networks of resident bacterial communities affect invasion resistance to the plant pathogen Ralstonia solanacearum in microcosms and in tomato plant rhizosphere. We find that bipartite resource competition networks are better predictors of invasion resistance compared with resident community diversity. Specifically, communities with a combination of stabilizing configurations (low nestedness and high connectance), and a clear niche overlap with the pathogen, reduce pathogen invasion success, constrain pathogen growth within invaded communities and have lower levels of diseased plants in greenhouse experiments. Bacterial resource competition network characteristics can thus be important in explaining positive diversity–invasion resistance relationships in bacterial rhizosphere communities. |
format | Online Article Text |
id | pubmed-4598729 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Pub. Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-45987292015-10-21 Trophic network architecture of root-associated bacterial communities determines pathogen invasion and plant health Wei, Zhong Yang, Tianjie Friman, Ville-Petri Xu, Yangchun Shen, Qirong Jousset, Alexandre Nat Commun Article Host-associated bacterial communities can function as an important line of defence against pathogens in animals and plants. Empirical evidence and theoretical predictions suggest that species-rich communities are more resistant to pathogen invasions. Yet, the underlying mechanisms are unclear. Here, we experimentally test how the underlying resource competition networks of resident bacterial communities affect invasion resistance to the plant pathogen Ralstonia solanacearum in microcosms and in tomato plant rhizosphere. We find that bipartite resource competition networks are better predictors of invasion resistance compared with resident community diversity. Specifically, communities with a combination of stabilizing configurations (low nestedness and high connectance), and a clear niche overlap with the pathogen, reduce pathogen invasion success, constrain pathogen growth within invaded communities and have lower levels of diseased plants in greenhouse experiments. Bacterial resource competition network characteristics can thus be important in explaining positive diversity–invasion resistance relationships in bacterial rhizosphere communities. Nature Pub. Group 2015-09-24 /pmc/articles/PMC4598729/ /pubmed/26400552 http://dx.doi.org/10.1038/ncomms9413 Text en Copyright © 2015, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Wei, Zhong Yang, Tianjie Friman, Ville-Petri Xu, Yangchun Shen, Qirong Jousset, Alexandre Trophic network architecture of root-associated bacterial communities determines pathogen invasion and plant health |
title | Trophic network architecture of root-associated bacterial communities determines pathogen invasion and plant health |
title_full | Trophic network architecture of root-associated bacterial communities determines pathogen invasion and plant health |
title_fullStr | Trophic network architecture of root-associated bacterial communities determines pathogen invasion and plant health |
title_full_unstemmed | Trophic network architecture of root-associated bacterial communities determines pathogen invasion and plant health |
title_short | Trophic network architecture of root-associated bacterial communities determines pathogen invasion and plant health |
title_sort | trophic network architecture of root-associated bacterial communities determines pathogen invasion and plant health |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4598729/ https://www.ncbi.nlm.nih.gov/pubmed/26400552 http://dx.doi.org/10.1038/ncomms9413 |
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